Abiusi, Emanuela
 Distribuzione geografica
Continente #
EU - Europa 429
NA - Nord America 377
AS - Asia 161
AF - Africa 10
Totale 977
Nazione #
US - Stati Uniti d'America 372
SE - Svezia 149
IT - Italia 89
DE - Germania 72
CN - Cina 67
TR - Turchia 32
IE - Irlanda 31
SG - Singapore 29
RU - Federazione Russa 20
UA - Ucraina 15
FI - Finlandia 13
FR - Francia 11
IR - Iran 11
CI - Costa d'Avorio 10
GB - Regno Unito 8
NL - Olanda 8
IN - India 7
HK - Hong Kong 6
KR - Corea 5
CZ - Repubblica Ceca 4
AT - Austria 2
CH - Svizzera 2
CR - Costa Rica 2
PK - Pakistan 2
CA - Canada 1
ES - Italia 1
HR - Croazia 1
IL - Israele 1
LI - Liechtenstein 1
MX - Messico 1
NO - Norvegia 1
PA - Panama 1
RS - Serbia 1
VN - Vietnam 1
Totale 977
Città #
Chandler 93
Ashburn 44
Dublin 29
Milan 25
New York 24
San Mateo 14
Singapore 13
Nanchang 12
Rome 12
Izmir 11
Abidjan 10
Jacksonville 10
Munich 10
Nanjing 10
Boston 9
Houston 9
Marseille 9
Wilmington 9
Cattolica 7
Helsinki 7
Princeton 7
Hong Kong 6
Norwalk 6
Old Bridge 6
Bremen 5
Dearborn 5
Fairfield 5
Seoul 5
Shenyang 5
Augusta 4
Beijing 4
Brno 4
Fremont 4
Naaldwijk 4
Nürnberg 4
Seattle 4
Alcamo 3
Amsterdam 3
Boardman 3
Caorle 3
Hefei 3
Lawrence 3
Moscow 3
Redwood City 3
Salò 3
Tehran 3
Tianjin 3
Trivandrum 3
University Park 3
Woodbridge 3
Ann Arbor 2
Bologna 2
Brixen 2
Cagliari 2
Cambridge 2
Ciserano 2
Cornate d'Adda 2
Hebei 2
Jinan 2
Kish 2
La Cruz 2
Lappeenranta 2
Los Angeles 2
Naples 2
Pisa 2
Taizhou 2
Turin 2
Vienna 2
Zurich 2
Andover 1
Atlanta 1
Busto Arsizio 1
Changchun 1
Changsha 1
Costa Mesa 1
Council Bluffs 1
Dallas 1
Edinburgh 1
Forest City 1
Frankfurt am Main 1
Fuzhou 1
Groningen 1
Guangzhou 1
Hangzhou 1
Hanoi 1
Juarez 1
Kocaeli 1
Kragujevac 1
Kunming 1
Leipzig 1
London 1
Madrid 1
Mountain View 1
Nuremberg 1
Nutley 1
Oslo 1
Pune 1
Ranica 1
Redmond 1
Saint Louis 1
Totale 556
Nome #
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study Running title: adult SMA biomarker study 148
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 89
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: Clues from a biomarker study 83
Neurological assessment of newborns with spinal muscular atrophy identified through neonatal screening 73
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: results of a phase IIb double-blind study of salbutamol 69
De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. 66
Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy 65
SMA-miRs (MiR-181a- 5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples 61
Longitudinal assessments in discordant twins with SMA 60
SMA-miRs (MiR-181a- 5p, -324-5p, and -451a) are overexpressed in spinal muscular atrophy skeletal muscle and serum samples 57
Experience of a 2-year spinal muscular atrophy NBS pilot study in Italy: towards specific guidelines and standard operating procedures for the molecular diagnosis 53
Plasma miR-151-3p as a candidate diagnostic biomarker for head and neck cancer: a cross-sectional study within the INHANCE consortium 48
Experience of a 2-year spinal muscular atrophy NBS pilot study in Italy: Towards specific guidelines and standard operating procedures for the molecular diagnosis 23
Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series 23
Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome? 18
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death 14
Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis 13
270th ENMC International Workshop: Consensus for SMN2 genetic analysis in SMA patients 10-12 March, 2023, Hoofddorp, the Netherlands 13
An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome 13
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita 11
Exome sequencing of ATP1A3-negative cases of alternating hemiplegia of childhood reveals SCN2A as a novel causative gene 8
Totale 1.008
Categoria #
all - tutte 5.361
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 5.361


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202058 17 2 1 0 4 5 15 2 3 1 5 3
2020/202135 0 3 0 4 4 1 9 1 5 4 4 0
2021/2022130 7 3 7 14 6 5 0 17 10 6 24 31
2022/2023330 56 42 13 30 36 21 39 37 28 7 14 7
2023/2024297 8 50 7 19 15 37 37 3 1 20 42 58
2024/202516 16 0 0 0 0 0 0 0 0 0 0 0
Totale 1.008